MTS cell proliferation assay is a colorimetric and high throughput method for sensitive quantification of viable cells, which is performed by adding the reagent into the cell culture media without the intermittent steps and requires no washing or solubilization step. The NAD(P)H-dependent dehydrogenase enzymes in metabolically active cells can cause the reduction of MTS tetrazolium compound and generate the colored formazan product that is soluble in cell culture media. Since viable cells can convert the MTS tetrazolium compound to the soluble and colored formazan product, color intensity can be significantly increased by measuring absorbance at 490-500 nm.
Figure 1. Structures of MTS tetrazolium salt and its formazan product (Anakok O F, et al., 2010).
Overview of MTS Cell Proliferation Assay Service
At Creative Proteomics, we provide MTS cell proliferation assay for the sensitive quantification of viable cells. The MTS cell proliferation assay involves culturing and treating cells, as well as adding MTS directly to the assay wells at a recommended ratio. Cells are incubated 1-4 hours and then absorbance is measured.
Figure 2. MTS cell proliferation assay procedure
At Creative Proteomics, we can apply our MTS cell proliferation assay to various fields, including but not limited:
The cell lines for assays should be provided by customers and our company can provide commonly used cell lines. This assay uses adherent and suspension cells.
If you want to know specific samples requirements, please feel free to contact us.
MTS cell proliferation assay is cost-effective and relatively easy to setup. At Creative Proteomics, many excellent and experienced experts will optimize the experimental protocol according to your requirement and guarantee the high-quality results for your research. As every project has different requirements, please contact our specialists to discuss your specific needs.
1. Anakok O F. Serrulatanes from Eremophila Neglecta: Their Spectrum of Antibacterial Activity, Cytotoxicity and Mode of Action. Research--University of South Australia, 2010.